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主要文件

810206P

Avanti

NBD Sphinganine

omega(7-nitro-2-1,3-benzoxadiazol-4-yl)(2S,3R)-2-aminooctadecane-1,3-diol, powder

别名:

D-erythro-sphinganine-N-NBD; NBD-dihydrosphingosine

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About This Item

经验公式(希尔记法):
C24H41N5O5
分子量:
479.61
MDL编号:
UNSPSC代码:
12352211
NACRES:
NA.25

方案

>99% (TLC)

表单

powder

包装

pkg of 1 × 100 μg ((810206P-100UG))
pkg of 1 × 250 μg (810206P-250ug)
pkg of 1 × 50 μg (810206P-50UG)

制造商/商品名称

Avanti Research - A Croda Brand 810206P

运输

dry ice

储存温度

−20°C

一般描述

Sphinganine, also called as dihydrosphingosine is a common sphingoid base in phospholipids.

应用

NBD Sphinganine or omega (7-nitro-2-1,3-benzoxadiazol-4-yl)(2S,3R)-2-aminooctadecane-1,3-diol is suitable for the analysis of the dihydrosphingosine (DHS) localization to endoplasmic reticulum for the activation of activating transcription factor 6 (ATF6) protein.
NBD Sphinganine or omega(7-nitro-2-1,3-benzoxadiazol-4-yl)(2S,3R)-2-aminooctadecane-1,3-diol is suitable for the analysis of the dihydrosphingosine (DHS) localization to endoplasmic reticulum for the activation of activating transcription factor 6 (ATF6) protein.

包装

5 mL Amber Glass Screw Cap Vial (810206P-100UG)
5 mL Amber Glass Screw Cap Vial (810206P-250UG)
5ML Glass Amber Screw Cap Vial (810206P-50UG)

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

No data available

闪点(°C)

No data available


历史批次信息供参考:

分析证书(COA)

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Arvin B Tam et al.
Developmental cell, 46(3), 327-343 (2018-08-08)
The unfolded protein response (UPR) is induced by proteotoxic stress of the endoplasmic reticulum (ER). Here we report that ATF6, a major mammalian UPR sensor, is also activated by specific sphingolipids, dihydrosphingosine (DHS) and dihydroceramide (DHC). Single mutations in a previously
Junliang Wan et al.
Journal of agricultural and food chemistry, 67(46), 12953-12961 (2019-10-23)
Most common sphingolipids are comprised of "typical" sphingoid bases (sphinganine, sphingosine, and structurally related compounds) and are produced via the condensation of l-serine with a fatty acyl-CoA by serine palmitoyltransferase. Some organisms, including mammals, also produce "atypical" sphingoid bases that

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